Kong Fanbing, Nicole White C, Xiao Xueyuan, Feng Youji, Xu Congjian, He Dacheng, Zhang Zhen, Yu Yinhua
Gynecology and Obstetrics Hospital of Fudan University, Shanghai, China.
Gynecol Oncol. 2006 Feb;100(2):247-53. doi: 10.1016/j.ygyno.2005.08.051. Epub 2005 Oct 17.
Early detection and monitoring the treatment remain the most important factors in improving long-term survival of ovarian cancer patients. New biomarkers that individually or in combination improve the diagnostic performance of existing tumor markers are critically needed. This study uses proteomic approaches to identify new biomarkers for detection and monitoring of ovarian cancer.
We analyzed protein profiles of three sets of sera using surface enhanced laser desorption and ionization time-of-light mass spectroscopy (SELDI-TOF-MS) on IMAC ProteinChip arrays and ProPeak software for bioinformatics data analysis. The first set of patients included 21 ovarian cancers, 18 benign diseases, and 20 normal patients. The second set included 32 ovarian cancers, 30 benign ovarian diseases, and 30 age-matched healthy controls. The third set included samples collected before and after chemotherapy from 18 ovarian cancer patients. All samples were collected at the Gynecology and Obstetrics Hospital of Fudan University in Shanghai, China. The datasets from low-intensity and high-intensity spectra were analyzed separately.
Seven peaks were selected for their contribution to the separation of ovarian cancers from controls using the first and second set of samples. The same dysregulation trends were confirmed for six of the seven peaks in independent validation using the third set of samples.
Using SELDI-TOF analysis of 195 unique specimens, we discovered with preliminary validation six distinct peaks that may potentially be useful in the detection and monitoring of ovarian cancer. Additional studies are required to determine the protein identities of these peaks and to further validate their performance as biomarkers.
早期检测和监测治疗仍然是提高卵巢癌患者长期生存率的最重要因素。迫切需要能够单独或联合使用以提高现有肿瘤标志物诊断性能的新生物标志物。本研究采用蛋白质组学方法来识别用于检测和监测卵巢癌的新生物标志物。
我们使用表面增强激光解吸电离飞行时间质谱(SELDI-TOF-MS)在IMAC蛋白芯片阵列上分析了三组血清的蛋白质谱,并使用ProPeak软件进行生物信息学数据分析。第一组患者包括21例卵巢癌患者、18例良性疾病患者和20例正常患者。第二组包括32例卵巢癌患者、30例良性卵巢疾病患者和30例年龄匹配的健康对照。第三组包括18例卵巢癌患者化疗前后采集的样本。所有样本均在中国上海复旦大学附属妇产科医院采集。对低强度和高强度光谱的数据集分别进行分析。
利用第一组和第二组样本,选择了7个对卵巢癌与对照分离有贡献的峰。在使用第三组样本进行的独立验证中,7个峰中的6个峰呈现相同的失调趋势。
通过对195个独特样本进行SELDI-TOF分析,我们初步验证发现了6个不同的峰,这些峰可能对卵巢癌的检测和监测有用。需要进一步研究来确定这些峰的蛋白质身份,并进一步验证它们作为生物标志物的性能。